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组胺和5-羟色胺——由H2和5-羟色胺受体介导的递质释放抑制作用

Histamine and 5-hydroxytryptamine-inhibition of transmitter release mediated by H2- and 5-hydroxytryptamine receptors.

作者信息

McGrath M A, Shepherd J T

出版信息

Fed Proc. 1978 Feb;37(2):195-8.

PMID:23966
Abstract

The vasodilatation caused by histamine and 5-hydroxytryptamine may be due, at least in part, to their inhibitory action on adrenergic neurotransmission. The evidence for this is as follows: 1) contractions of isolated canine vascular strips caused by sympathetic nerve stimulation are depressed by these substances whereas contractions caused by norepinephrine are either unchanged or augmented; 2) histamine and 5-hydroxytryptamine inhibit the release of norepinephrine evoked by sympathetic nerve stimulation of isolated vascular strips previously incubated with the labeled transmitter. This inhibitory effect can be demonstrated using concentrations of the substinces less than those required to affect the smooth muscle cells directly. By contrast, neither histamine nor 5-hydroxytryptamine inhibits the displacement of neuronal norepinephrine by tyramine, suggesting that these substances interfere with the exocytotic process. Additional studies have identified the histamine-H2 receptor as the probable mediator of this prejunctional action of histamine, whereas the nature of the receptor for 5-hydroxytryptamine remains to be clarified.

摘要

组胺和5-羟色胺引起的血管舒张至少部分可能归因于它们对肾上腺素能神经传递的抑制作用。支持这一观点的证据如下:1)这些物质会抑制交感神经刺激引起的离体犬血管条收缩,而对去甲肾上腺素引起的收缩则无影响或使其增强;2)组胺和5-羟色胺抑制交感神经刺激预先用标记递质孵育的离体血管条所诱发的去甲肾上腺素释放。使用低于直接影响平滑肌细胞所需浓度的这些物质就能证明这种抑制作用。相比之下,组胺和5-羟色胺均不抑制酪胺对神经元去甲肾上腺素的置换,这表明这些物质干扰了胞吐过程。进一步的研究已确定组胺-H2受体可能是组胺这种突触前作用的介质,而5-羟色胺的受体性质仍有待阐明。

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